EP0896739A1 - Diode-addressed colour display with lanthanoid phosphors - Google Patents
Diode-addressed colour display with lanthanoid phosphorsInfo
- Publication number
- EP0896739A1 EP0896739A1 EP98904317A EP98904317A EP0896739A1 EP 0896739 A1 EP0896739 A1 EP 0896739A1 EP 98904317 A EP98904317 A EP 98904317A EP 98904317 A EP98904317 A EP 98904317A EP 0896739 A1 EP0896739 A1 EP 0896739A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- diode
- carboxylic acid
- phenanthroline
- oxide
- acetylacetonate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 229910052747 lanthanoid Inorganic materials 0.000 title description 4
- 150000002602 lanthanoids Chemical class 0.000 title description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 24
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 21
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims abstract description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000012965 benzophenone Substances 0.000 claims abstract description 7
- BAEVILLEIGDCDN-UHFFFAOYSA-N 4-chloro-1,10-phenanthroline Chemical compound C1=CC2=CC=CN=C2C2=C1C(Cl)=CC=N2 BAEVILLEIGDCDN-UHFFFAOYSA-N 0.000 claims abstract description 6
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims abstract description 6
- LRMLWYXJORUTBG-UHFFFAOYSA-N dimethylphosphorylmethane Chemical compound CP(C)(C)=O LRMLWYXJORUTBG-UHFFFAOYSA-N 0.000 claims abstract description 6
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 claims abstract description 6
- ZSSWXNPRLJLCDU-UHFFFAOYSA-N 1-diethylphosphorylethane Chemical compound CCP(=O)(CC)CC ZSSWXNPRLJLCDU-UHFFFAOYSA-N 0.000 claims abstract description 5
- POEOLRMDMUNLPY-UHFFFAOYSA-N 2,3-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC2=CC=C(C=CC=N3)C3=C2N=C1C1=CC=CC=C1 POEOLRMDMUNLPY-UHFFFAOYSA-N 0.000 claims abstract description 5
- QBHDSQZASIBAAI-UHFFFAOYSA-N 4-acetylbenzoic acid Chemical compound CC(=O)C1=CC=C(C(O)=O)C=C1 QBHDSQZASIBAAI-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- NAMDIHYPBYVYAP-UHFFFAOYSA-N 1-methoxy-2-(2-methoxyethoxy)ethane Chemical compound COCCOCCOC.COCCOCCOC NAMDIHYPBYVYAP-UHFFFAOYSA-N 0.000 claims description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- 239000006104 solid solution Substances 0.000 claims description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 abstract 2
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical group C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- -1 CH¿3? Chemical group 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000009102 absorption Effects 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000003822 epoxy resin Substances 0.000 description 5
- 239000003446 ligand Substances 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 238000006862 quantum yield reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- IFQUPKAISSPFTE-UHFFFAOYSA-N 4-benzoylbenzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C(=O)C1=CC=CC=C1 IFQUPKAISSPFTE-UHFFFAOYSA-N 0.000 description 3
- 238000000695 excitation spectrum Methods 0.000 description 3
- 229910052692 Dysprosium Inorganic materials 0.000 description 2
- 229910052693 Europium Inorganic materials 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 229910052772 Samarium Inorganic materials 0.000 description 2
- 229910052771 Terbium Inorganic materials 0.000 description 2
- 229910052775 Thulium Inorganic materials 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 description 2
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910021644 lanthanide ion Inorganic materials 0.000 description 1
- 150000002601 lanthanoid compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- 229960000368 sulisobenzone Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- FRNOGLGSGLTDKL-UHFFFAOYSA-N thulium atom Chemical compound [Tm] FRNOGLGSGLTDKL-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
- H01J29/02—Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
- H01J29/10—Screens on or from which an image or pattern is formed, picked up, converted or stored
- H01J29/18—Luminescent screens
- H01J29/20—Luminescent screens characterised by the luminescent material
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/182—Metal complexes of the rare earth metals, i.e. Sc, Y or lanthanide
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
- H01L33/50—Wavelength conversion elements
- H01L33/501—Wavelength conversion elements characterised by the materials, e.g. binder
- H01L33/502—Wavelength conversion materials
Definitions
- Diode-addressed color display with lanthanide phosphors Diode-addressed color display with lanthanide phosphors.
- the invention relates to a diode-addressed color display with a UV diode and a phosphor for illuminated displays, lights, solid-state image intensifiers, screens and monitors and others.
- Color displays for illuminated displays, luminaires, solid state amplifiers, screens and monitors are intended to reproduce color images in true color.
- this object is achieved in that the entire color information of a colored image is represented by information about the three primary colors red, green and blue.
- Additive color mixing can be used to produce any color or white from the three primary colors. This principle is used both by the conventional color television set with a tube from Braunschweig and by the various flat screen technologies such as plasma screens,
- Electroluminescent screen and LCD displays There are also color displays on the market in which the triple color red, green, blue is generated by diode arrays with red, green and blue emitting semiconductor diodes.
- the color-true image reproduction in particular the color-pure reproduction of green and blue, is problematic.
- the development of UV-emitting semiconductor diodes has expanded the possibilities for true-color image reproduction for diode-addressed color displays, since theoretically any color of visible light can be generated from UV light.
- phosphors are used which absorb the UV light and emit it again with a wavelength in the visible range. For this conversion of the UV light into the visible range, it is known to use inorganic pigments as phosphors. For example, it's off
- Such a color display is characterized by a high intrinsic emission quantum yield and a ligand-centered absorption in the near UV and the short-wave visible range between 320 and 450 nm with high extinction coefficients.
- the UV absorption has its maximum at 390 to 320 nm. According to photophysical considerations, these two phosphor properties are actually mutually exclusive. Surprisingly, however, it has been shown that phosphors of the composition LnL 3 X 2 meet both criteria.
- the phosphors according to the invention with the "antenna molecules" L which contain benzophenone or acetophenone as structural elements, have many times higher absorptions than classic phosphors.
- a variation of the ligands L allows the almost linear, independent introduction of high absorptions at different wavelengths into the lanthanoid compounds. Concentration quenching, a general problem with classic phosphors with a high activator concentration, is not observed with the phosphors according to the invention.
- the phosphors according to the invention are molecular compounds and therefore generally readily soluble in polar organic solvents. Their properties can therefore be easily examined in solution and the test results can be transferred to the solid state. The solubility in organic solvents also allows new design concepts for diode-addressed color displays.
- the diode-addressed color display comprises a transparent polymeric coating which contains the phosphorus of the composition LnL 3 X 2 in solid solution.
- the coating is transparent because the light is not scattered on the dissolved phosphor particles.
- the phosphors containing europium or samarium convert the UV radiation into visible red light.
- the terbium-containing phosphor converts to green light, the thulium-containing to blue and the dysprosium-containing to blue-yellow mixed light.
- a color display according to the invention consists of the
- the transparent coating can contain, for example, the phosphorus in a solid solution in a transparent matrix made of polyacrylate, polystyrene, epoxy resin or another polymer.
- LEDs are usually cast in epoxy housings, with the cast-on lens made of epoxy resin serving to improve the coupling out of the light from the diode.
- the phosphor can be applied as a contact layer between the actual diode and the epoxy resin dome. It can also be applied as a coating on the outside of the epoxy resin dome.
- the phosphorus is mixed with the epoxy resin and forms a solid solution with it.
- the diode array can be covered by a glass plate which is printed with fluorescent triplets, each with a red, green and blue glowing dot.
- the red glowing dot contains LnL 3 X 2 as phosphor.
- the UV diode is in particular a UV diode made of InGaN or GaN and has its emission maximum between 370 and 410 nm with a half width FWHM ⁇ 50 nm.
- These complex coordination compounds of the lanthanoids europium, terbium, thulium, dysprosium and samarium contain Eu 3 + , Tb 3 + , Tm 3 + , Dys 3 + and Sm 3 + as the metal center, benzophenone-4-carboxylic acid or its derivatives or benzophenone-4 -acety lacetonate or its derivatives as charged ligands and phenanthroline, 1/2 diphenylphenanthroline, 1/2 4-Cl-phenanthroline, 1/2 bipyridine, 1/2 ethylenediamine, triphenylphosphine oxide, trimethylphosphine oxide, triethylphosphine oxide, 1/2 diethylene glycol dimethyl ether ( diglyme) or ethanol as neutral ligands.
- These coordination compounds have strong optical intraligand transitions and, in addition to absorbing the chelate ligands, are also effective as light antennas.
- the primary excitation by UV radiation leads to a ligand-centered excited state, the energy of which is transferred to the lanthanide ion in a subsequent step and leads to light emission there.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19708562 | 1997-03-04 | ||
DE19708562 | 1997-03-04 | ||
DE19800983 | 1998-01-14 | ||
DE19800983A DE19800983A1 (en) | 1997-03-04 | 1998-01-14 | Diode-addressed color display with lanthanide phosphors |
PCT/IB1998/000268 WO1998039807A1 (en) | 1997-03-04 | 1998-03-03 | Diode-addressed colour display with lanthanoid phosphors |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0896739A1 true EP0896739A1 (en) | 1999-02-17 |
Family
ID=26034454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98904317A Withdrawn EP0896739A1 (en) | 1997-03-04 | 1998-03-03 | Diode-addressed colour display with lanthanoid phosphors |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0896739A1 (en) |
WO (1) | WO1998039807A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6165631A (en) * | 1997-03-04 | 2000-12-26 | U.S. Philips Corporation | Diode-addressed color display with lanthanoid phosphors |
US7871713B2 (en) | 1998-12-25 | 2011-01-18 | Konica Corporation | Electroluminescent material, electroluminescent element and color conversion filter |
US6656608B1 (en) | 1998-12-25 | 2003-12-02 | Konica Corporation | Electroluminescent material, electroluminescent element and color conversion filter |
DE10036940A1 (en) | 2000-07-28 | 2002-02-07 | Patent Treuhand Ges Fuer Elektrische Gluehlampen Mbh | Luminescence conversion LED |
DE10105800B4 (en) | 2001-02-07 | 2017-08-31 | Osram Gmbh | Highly efficient phosphor and its use |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5006503A (en) * | 1990-03-13 | 1991-04-09 | Eastman Kodak Company | Thermally-transferable fluorescent europium complexes |
JPH05152609A (en) * | 1991-11-25 | 1993-06-18 | Nichia Chem Ind Ltd | Light emitting diode |
-
1998
- 1998-03-03 EP EP98904317A patent/EP0896739A1/en not_active Withdrawn
- 1998-03-03 WO PCT/IB1998/000268 patent/WO1998039807A1/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9839807A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1998039807A1 (en) | 1998-09-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0907970B1 (en) | White light-emitting diode | |
DE60312733T2 (en) | LIGHTING DEVICE WITH RADIATION SOURCE AND FLUORESCENT MATERIAL | |
EP1699899B9 (en) | Luminous substance and light source comprising such a luminous substance | |
DE60130762T2 (en) | ELECTROLUMINESCENT MATERIALS AND ARTICLES FROM A POLYMERMATRIX | |
EP1123337B1 (en) | Conjugated polymers containing 2,7 fluorenyl units with improved properties | |
EP1970970B1 (en) | Lighting unit with at least one LED as light source | |
EP1206802B1 (en) | Led-based white-light emitting lighting unit | |
DE112007000656B4 (en) | Phosphor, method for producing the same, and light-emitting devices using the same | |
DE112009000181B4 (en) | Process for the production of white light emitting material | |
DE112005002737T5 (en) | New class of bridged biphenyl polymers | |
KR20170069211A (en) | Module for image display devices, and image display device | |
DE60014038T2 (en) | ELEKTROLUMINESZENZMATERIALEN | |
TWI405359B (en) | White light emitting diodes and the use of its backlight and liquid crystal display device | |
DE112007002622T5 (en) | Aluminate phosphor containing divalent metal elements, making the same and light-emitting devices using the same | |
KR101821917B1 (en) | Liquid crystal display device and method for producing same | |
DE102008038249A1 (en) | alpha-sialon phosphor | |
DE112006000379T5 (en) | Arylene polymers with a large band gap | |
DE19802046A1 (en) | Diode-addressed color display with molecular phosphor | |
DE112007001712T5 (en) | Silicon-containing phosphor for LED, its manufacture and light-emitting devices using the same | |
US6165631A (en) | Diode-addressed color display with lanthanoid phosphors | |
DE112011104395T5 (en) | White afterglow fluorescent mixture or layer structure | |
EP0227980A2 (en) | Fluorescent aroxysubstituted 3,4,9,10-perylenetetracarboxylic acid-diimides and their use for the concentration of lights in small areas | |
WO1998039807A1 (en) | Diode-addressed colour display with lanthanoid phosphors | |
DE19800983A1 (en) | Diode-addressed color display with lanthanide phosphors | |
DE102004060708B4 (en) | Red fluorescent material and white light emitting diodes using red fluorescent material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB |
|
17P | Request for examination filed |
Effective date: 19990311 |
|
RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: PHILIPS CORPORATE INTELLECTUAL PROPERTY GMBH Owner name: KONINKLIJKE PHILIPS ELECTRONICS N.V. |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: PHILIPS CORPORATE INTELLECTUAL PROPERTY GMBH Owner name: KONINKLIJKE PHILIPS ELECTRONICS N.V. |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: PHILIPS INTELLECTUAL PROPERTY & STANDARDS GMBH Owner name: KONINKLIJKE PHILIPS ELECTRONICS N.V. |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Effective date: 20070927 |